Canonical Allele Identifier: CA280601577

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191015C>T , CM000678.2:g.31191015C>T	GRCh38
NC_000016.9:g.31202336C>T , CM000678.1:g.31202336C>T	GRCh37
NC_000016.8:g.31109837C>T	NCBI36
NG_012889.2:g.15884C>T , LRG_655:g.15884C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.1446C>T MANE Select	NP_004951.1:p.Gly482=
ENST00000254108.12:c.1446C>T MANE Select	ENSP00000254108.8:p.Gly482=
NM_001170634.1:c.1443C>T	NP_001164105.1:p.Gly481=
NM_001170937.1:c.1434C>T	NP_001164408.1:p.Gly478=
NM_004960.3:c.1446C>T , LRG_655t1:c.1446C>T	NP_004951.1:p.Gly482=
NR_028388.2:n.1516C>T
ENST00000254108.11:c.1446C>T	ENSP00000254108.7:p.Gly482=
ENST00000380244.7:c.1443C>T	ENSP00000369594.3:p.Gly481=
ENST00000474990.5:n.740C>T
ENST00000483853.1:n.523C>T
ENST00000487509.6:n.4621C>T
ENST00000566605.5:c.*619C>T	ENSP00000455073.1:n.*619C>T
ENST00000568685.1:c.1449C>T	ENSP00000455282.1:p.Gly483=
ENST00000569760.5:n.337C>T
XM_005255233.3:c.831C>T	XP_005255290.1:p.Gly277=
XM_005255233.5:c.831C>T	XP_005255290.1:p.Gly277=
XM_011545781.1:c.1440C>T	XP_011544083.1:p.Gly480=
XM_011545782.1:c.831C>T	XP_011544084.1:p.Gly277=
XM_011545782.2:c.831C>T	XP_011544084.1:p.Gly277=
XM_024450221.1:c.1437C>T	XP_024305989.1:p.Gly479=